Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2753960
rs2753960
2 6 31795067 missense variant G/T snv 0.43 0.36 0.700 1.000 1 2016 2016
dbSNP: rs9469054
rs9469054
2 6 31793286 intron variant G/A snv 3.5E-02 0.700 1.000 1 2016 2016